Accessible Tetrathiafulvalene Moieties in a 3D Covalent Organic Framework for Enhanced Near‐Infrared Photo‐Thermal Conversion and Photo‐Electrical Response

Redox‐active tetrathiafulvalene (TTF)‐based covalent organic frameworks (COFs) exhibit distinctive electrochemical and photoelectrical properties, but their prevalent two‐dimensional (2D) structure with densely packed TTF moieties limits the accessibility of redox center and constrains their potential applications. To overcome this challenge, an 8‐connected TTF linker (TTF‐8CHO) is designed as a new building block for the construction of three‐dimensional (3D) COFs. This approach led to the successful synthesis of a 3D COF with the bcu topology, designated as TTF‐8CHO‐COF. In comparison to its 2D counterpart employing a 4‐connected TTF linker, the 3D COF design enhances access to redox sites, facilitating controlled oxidation by I2 or Au3+ to tune physical properties. When irradiated with a 0.7 W cm−2 808 nm laser, the oxidized 3D COF samples (IX−${\mathrm{I}}_{\mathrm{X}}^{-}$@TTF‐8CHO‐COF and Au NPs@TTF‐8CHO‐COF) demonstrated rapid temperature increases of 239.3 and 146.1 °C, respectively, which surpassed those of pristine 3D COF (65.6 °C) and the 2D COF counterpart (6.4 °C increment after I2 treatment). Furthermore, the oxidation of the 3D COF heightened its photoelectrical responsiveness under 808 nm laser irradiation. This augmentation in photothermal and photoelectrical response can be attributed to the higher concentration of TTF·+ radicals generated through the oxidation of well‐exposed TTF moieties. A new red‐ox active three‐dimensional (3D) covalent organic framework (COF) is synthesized by a tetrathiafulvalene (TTF)‐based 8‐connected building block. Because of the generations of stable TTF·+ states after oxidization, the systems show well‐tunable physical proprieties for near‐infrared photo‐thermal conversion and photo‐electrical response.